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90619-86-6

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90619-86-6 Usage

Class of Organic Compounds

Belongs to the class of 2-thiophenecarboxylic acids and derivatives.

Derivation

It is a derivative of thiophene, which is a five-membered aromatic ring with one sulfur atom.

Usage in Production

Used in the production of various pharmaceuticals, dyes, and agrochemicals.

Industrial Applications

Used as a building block in the synthesis of other organic compounds and has various industrial applications.

Raw Material Usage

Utilized as a raw material in the production of fine chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 90619-86-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,6,1 and 9 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 90619-86:
(7*9)+(6*0)+(5*6)+(4*1)+(3*9)+(2*8)+(1*6)=146
146 % 10 = 6
So 90619-86-6 is a valid CAS Registry Number.

90619-86-6 Well-known Company Product Price

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  • Aldrich

  • (708305)  5-Hexyl-2-thiophenecarboxylicacid  97%

  • 90619-86-6

  • 708305-1G

  • 952.38CNY

  • Detail

90619-86-6SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-hexylthiophene-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 2-Thiophenecarboxylic acid,5-hexyl

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:90619-86-6 SDS

90619-86-6Relevant articles and documents

Effect of alkyl chain and linking units on mesophase transitions and molecular order of rod-like thiophene mesogens: 13C NMR investigation

Santhosh Kumar Reddy,Lobo, Nitin P.,Narasimhaswamy

supporting information, p. 598 - 612 (2017/12/28)

Thermotropic liquid crystals with π-conjugated cores are increasingly witnessed due to their promising optoelectronic and optophotonic properties. As π-conjugated mesogens are often realized by direct linking of the rings of the core, the mesophase transitions are usually modulated by inserting the required alkyl/alkoxy chains either at a terminal or lateral location. In this work, five mesogens in which thiophene and two phenyl rings are common in the core unit with terminal alkyl/alkoxy chains are investigated to probe the influence of (a) a terminal alkyl chain on the mesophase characteristics, (b) the linking units on the mesophase range and (c) the disparity of thiophene orientational constraints. The mesophase properties reveal that whenever the alkyl chain is located at one end of the molecule, polymesomorphism is observed. The XRD studies reveal layer ordering typical of smectic mesophases with lower temperature and higher order phases, namely SmB and CrE phases. A detailed 13C NMR study of the mesogens in the liquid crystalline phase indicates that the order parameters are governed by the nature of the substitution of thiophene and its linkage with two phenyl rings. Importantly, the 13C NMR data of the terminal chains in the liquid crystalline phase are compared with the recently reported thiophene mesogen in which the n-hexyl chain is located at the lateral position and completely different orientation characteristics were found for the terminal versus lateral chains.

Mesomorphic compound, liquid crystal composition, liquid crystal device, display apparatus and display method

-

, (2008/06/13)

A mesomorphic compound represented by the following formula (I): STR1 wherein R1 and R2 respectively denote a linear or branched alkyl group having 1-18 carbon atoms capable of including one or two or more non-neighboring methylene groups which can be replaced with STR2 wherein X denotes halogen; X1 and X2 respectively denote STR3 Z1 denotes STR4 A1 denotes a single bond, STR5 and Y1 and Y2 respectively denote H, F, Cl, Br, --CH3 or --CF3 with the proviso that Y1 and Y2 are not simultaneously H. The mesomorphic compound is effective for providing a ferroelectric liquid crystal composition showing an improved low-temperature operation characteristic and a decreased temperature-dependence of response speed.

Mesomorphic compound, liquid crystal composition and liquid crystal device using same

-

, (2008/06/13)

A mesomorphic compound represented by the following formula (I): STR1 wherein R1 and R2 respectively denote a linear or branched alkyl group having 1-18 carbon atoms capable of having a substituent; X denotes any one of a single bond, --O--, STR2 Y denotes STR3 or --CH2 O--; and Z denotes any one of --O--, STR4 .

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